generalized dystonia

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Results for "generalized dystonia": 504 gene sets

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generalized dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease generalized dystonia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
generalized dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease generalized dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
generalized dystonia Gene Set From HPO Gene-Disease Associations genes associated with the generalized dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Generalized Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Generalized dystonia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Generalized dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset generalized limb-onset dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset generalized limb-onset dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypermanganesemia with dystonia, polycythemia and cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 24 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant torsion dystonia 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant torsion dystonia 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonic dystonia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myoclonic dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile-onset dystonia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile-onset dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 25 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 6, torsion Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 6, torsion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 5, Dopa-responsive type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 5, Dopa-responsive type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 3, torsion, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 3, torsion, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dystonia 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dystonia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Infantile Parkinsonism-dystonia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Infantile Parkinsonism-dystonia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Parkinsonism-Dystonia, Infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Parkinsonism-Dystonia, Infantile from the curated CTD Gene-Disease Associations dataset.
Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.
Dystonia musculorum deformans type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia musculorum deformans type 2 from the curated CTD Gene-Disease Associations dataset.
Dystonia 13, Torsion Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia 13, Torsion from the curated CTD Gene-Disease Associations dataset.
Dystonia musculorum deformans type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia musculorum deformans type 1 from the curated CTD Gene-Disease Associations dataset.
Torsion dystonia 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Torsion dystonia 7 from the curated CTD Gene-Disease Associations dataset.
Dystonia 17, Torsion, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia 17, Torsion, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Dystonia 15, myoclonic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia 15, myoclonic from the curated CTD Gene-Disease Associations dataset.
LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY from the curated CTD Gene-Disease Associations dataset.
Dystonia 12 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia 12 from the curated CTD Gene-Disease Associations dataset.
Myoclonic dystonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myoclonic dystonia from the curated CTD Gene-Disease Associations dataset.
Familial paroxysmal dystonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Familial paroxysmal dystonia from the curated CTD Gene-Disease Associations dataset.
Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency from the curated CTD Gene-Disease Associations dataset.
Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypermanganesemia with Dystonia Polycythemia and Cirrhosis from the curated CTD Gene-Disease Associations dataset.
Juvenile-onset dystonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile-onset dystonia from the curated CTD Gene-Disease Associations dataset.
Dystonia 3, Torsion, X-Linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia 3, Torsion, X-Linked from the curated CTD Gene-Disease Associations dataset.
Dystonia 6, torsion Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia 6, torsion from the curated CTD Gene-Disease Associations dataset.
Dystonia, Dopa-responsive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia, Dopa-responsive from the curated CTD Gene-Disease Associations dataset.
Cervical Dystonia, Primary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cervical Dystonia, Primary from the curated CTD Gene-Disease Associations dataset.
Dystonia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia from the curated CTD Gene-Disease Associations dataset.
dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dystonia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
deafness dystonia syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease deafness dystonia syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
dystonia Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease dystonia in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cranio-facial dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cranio-facial dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
focal dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease focal dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
deafness dystonia syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease deafness dystonia syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dystonia, primary torsion Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia, primary torsion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complex regional pain syndromes; dystonia; Gene Set From GAD Gene-Disease Associations genes associated with the disease complex regional pain syndromes; dystonia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myoclonus dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease myoclonus dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia; Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
idiopathic torsion dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease idiopathic torsion dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia, primary Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia, primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome deletion; dystonia; myoclonus Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome deletion; dystonia; myoclonus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cervical dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease cervical dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia, cervical Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia, cervical in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia, focal Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia, focal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blepharospasm; dystonia; dystonic disorders; torticollis Gene Set From GAD Gene-Disease Associations genes associated with the disease blepharospasm; dystonia; dystonic disorders; torticollis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia, early onset primary Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia, early onset primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
akathisia, drug-induced; dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease akathisia, drug-induced; dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia; psychomotor disorders; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonia; psychomotor disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
focal dystonia Gene Set From GAD Gene-Disease Associations genes associated with the disease focal dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonia Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term dystonia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Musician's dystonia Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Musician's dystonia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
craniofacial dystonia Gene Set From HPO Gene-Disease Associations genes associated with the craniofacial dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb dystonia Gene Set From HPO Gene-Disease Associations genes associated with the limb dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
axial dystonia Gene Set From HPO Gene-Disease Associations genes associated with the axial dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
oromandibular dystonia Gene Set From HPO Gene-Disease Associations genes associated with the oromandibular dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dystonia Gene Set From HPO Gene-Disease Associations genes associated with the dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
paroxysmal dystonia Gene Set From HPO Gene-Disease Associations genes associated with the paroxysmal dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
laryngeal dystonia Gene Set From HPO Gene-Disease Associations genes associated with the laryngeal dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
torsion dystonia Gene Set From HPO Gene-Disease Associations genes associated with the torsion dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
focal dystonia Gene Set From HPO Gene-Disease Associations genes associated with the focal dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Dystonia Musculorum Deformans Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dystonia Musculorum Deformans phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Dystonia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Dystonia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
dystonia Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dystonia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dystonia 6, torsion Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 6, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-17, primary torsion Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-17, primary torsion phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-parkinsonism, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-parkinsonism, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 4, torsion, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 4, torsion, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 9 Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 13, torsion Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 13, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-12 Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-12 phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 21 Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 21 phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 24 Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 24 phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 25 Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 25 phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, primary cervical Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, primary cervical phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, myoclonic Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, myoclonic phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, dystonia, and cerebral hypomyelination Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, dystonia, and cerebral hypomyelination phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-1, torsion Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-1, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.
{dystonia-1, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {dystonia-1, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
parkinsonism-dystonia, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the parkinsonism-dystonia, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-7, torsion Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-7, torsion phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-11, myoclonic Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-11, myoclonic phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, juvenile-onset Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia-15, myoclonic Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia-15, myoclonic phenotype from the curated OMIM Gene-Disease Associations dataset.
hypermanganesemia with dystonia, polycythemia, and cirrhosis Gene Set From OMIM Gene-Disease Associations genes associated with the hypermanganesemia with dystonia, polycythemia, and cirrhosis phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia 16 Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia 16 phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, dopa-responsive, due to sepiapterin reductase deficiency Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, dopa-responsive, due to sepiapterin reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy with dystonia and motor neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with dystonia and motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, early-onset atypical, with myoclonic features Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, early-onset atypical, with myoclonic features phenotype from the curated OMIM Gene-Disease Associations dataset.
dystonia, dopa-responsive, with or without hyperphenylalaninemia Gene Set From OMIM Gene-Disease Associations genes associated with the dystonia, dopa-responsive, with or without hyperphenylalaninemia phenotype from the curated OMIM Gene-Disease Associations dataset.
Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile-Onset Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile-Onset Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myoclonic Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myoclonic Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Onset Torsion Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Onset Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Musician'S Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Musician'S Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Segmental Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Segmental Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dopa-Responsive Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dopa-Responsive Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Isolated Cervical Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Isolated Cervical Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fragments Of Torsion Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fragments Of Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Non-Familial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Non-Familial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symptomatic Torsion Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symptomatic Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cervical Dystonia, Primary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cervical Dystonia, Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Laryngeal Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Laryngeal Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Craniofacial Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Craniofacial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leber Optic Atrophy And Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leber Optic Atrophy And Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Torsion Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Torsion Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Torsion Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Myoclonic Epilepsy With Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Myoclonic Epilepsy With Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cervical Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cervical Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Oromandibular Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Oromandibular Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Lingual Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lingual Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axial Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axial Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Acute Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Acute Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Leg Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Leg Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Other Dystonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Other Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
dystonia Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the dystonia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5619081 Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5619081 pathway from the Reactome Pathways 2024 dataset.
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5660724 Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)_5660724 pathway from the Reactome Pathways 2024 dataset.
Dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Dystonia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Focal dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Focal dystonia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked dystonia-parkinsonism Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked dystonia-parkinsonism from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Torsion dystonia 6 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Torsion dystonia 6 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
dystonia, DOPA-responsive Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease dystonia, DOPA-responsive from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Dystonia 12 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Dystonia 12 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Dystonia 16 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Dystonia 16 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multifocal dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multifocal dystonia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
deafness-dystonia-optic neuronopathy syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease deafness-dystonia-optic neuronopathy syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hypermanganesemia with dystonia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hypermanganesemia with dystonia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Leber hereditary optic neuropathy and dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leber hereditary optic neuropathy and dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
deafness-dystonia-optic neuronopathy syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease deafness-dystonia-optic neuronopathy syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Focal hand dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Focal hand dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multifocal dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multifocal dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Oromandibular dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Oromandibular dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Segmental dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Segmental dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile parkinsonism-dystonia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile parkinsonism-dystonia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 16 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spasmodic dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spasmodic dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypermanganesemia with dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypermanganesemia with dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypermanganesemia with dystonia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypermanganesemia with dystonia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cervical dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cervical dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Torsion dystonia 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Torsion dystonia 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked dystonia-parkinsonism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked dystonia-parkinsonism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 28, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 28, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Torsion dystonia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Torsion dystonia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
dystonia, DOPA-responsive Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease dystonia, DOPA-responsive in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset dystonia with optic atrophy and basal ganglia abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset dystonia with optic atrophy and basal ganglia abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myoclonic dystonia 26 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myoclonic dystonia 26 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 27 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 27 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myoclonic dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myoclonic dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hypermanganesemia with dystonia 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hypermanganesemia with dystonia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
deafness, dystonia, and cerebral hypomyelination Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease deafness, dystonia, and cerebral hypomyelination in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myoclonic dystonia 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myoclonic dystonia 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 35, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 35, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cranio-facial dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cranio-facial dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 32 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 32 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Torsion dystonia 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Torsion dystonia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 25 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 25 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Torsion dystonia 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Torsion dystonia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 24 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 24 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Torsion dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Torsion dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Paroxysmal dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Paroxysmal dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myoclonic dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myoclonic dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive DOPA responsive dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive DOPA responsive dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dopa-responsive dystonia due to sepiapterin reductase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dopa-responsive dystonia due to sepiapterin reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Developmental malformations-deafness-dystonia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Developmental malformations-deafness-dystonia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Parkinsonism-dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Parkinsonism-dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neurodegenerative illness progressing to crippling dystonia and death Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neurodegenerative illness progressing to crippling dystonia and death phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Limb dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Limb dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dopa-responsive dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dopa-responsive dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myoclonus-dystonia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myoclonus-dystonia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked dystonia-parkinsonism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked dystonia-parkinsonism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Deafness dystonia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Deafness dystonia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TSPOAP1-related Dystonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TSPOAP1-related Dystonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Musician's dystonia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Musician's dystonia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Congenital generalized lipodystrophy type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital generalized lipodystrophy type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyrotropin-releasing hormone resistance, generalized Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thyrotropin-releasing hormone resistance, generalized phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Lipodystrophy, congenital generalized, type 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Lipodystrophy, congenital generalized, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyroid hormone resistance, generalized, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone resistance, generalized, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized arterial calcification of infancy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized arterial calcification of infancy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Thyroid hormone resistance, generalized, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone resistance, generalized, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized dominant dystrophic epidermolysis bullosa Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized dominant dystrophic epidermolysis bullosa phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy with febrile seizures plus 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy with febrile seizures plus 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pustular psoriasis, generalized Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pustular psoriasis, generalized phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy with febrile seizures plus, type 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy with febrile seizures plus, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy with febrile seizures plus, type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy with febrile seizures plus, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy with febrile seizures plus, type 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy with febrile seizures plus, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Glucocorticoid resistance, generalized Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Glucocorticoid resistance, generalized phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Generalized epilepsy and paroxysmal dyskinesia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Generalized from the curated CTD Gene-Disease Associations dataset.
Thyroid Hormone Resistance, Generalized, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Resistance, Generalized, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 6 from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Idiopathic Generalized Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Idiopathic Generalized from the curated CTD Gene-Disease Associations dataset.
Thyroid Hormone Resistance, Generalized, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Resistance, Generalized, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy and Paroxysmal Dyskinesia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy and Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 1 from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 3 from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 4 from the curated CTD Gene-Disease Associations dataset.
Hypertrichosis congenital generalized X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertrichosis congenital generalized X-linked from the curated CTD Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, Type 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Generalized Epilepsy With Febrile Seizures Plus, Type 2 from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized, Type 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 3 from the curated CTD Gene-Disease Associations dataset.
Lipodystrophy, Congenital Generalized, Type 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 4 from the curated CTD Gene-Disease Associations dataset.
Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia from the curated CTD Gene-Disease Associations dataset.
congenital generalized lipodystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital generalized lipodystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
congenital generalized lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
generalized atherosclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease generalized atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
epilepsy with generalized tonic-clonic seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease epilepsy with generalized tonic-clonic seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
idiopathic generalized epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease idiopathic generalized epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
generalized epilepsy with febrile seizures plus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease generalized epilepsy with febrile seizures plus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
generalized anxiety disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease generalized anxiety disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glucose tolerance; lipids; atherosclerosis, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease glucose tolerance; lipids; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hiv; atherosclerosis, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease hiv; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis, generalized; vascular disease Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis, generalized; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, absence; epilepsy, generalized; epilepsy, reflex; myoclonic epilepsy, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intima-media thickness; atherosclerosis, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease intima-media thickness; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, absence; epilepsy, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, absence; epilepsy, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome deletion; epilepsy, generalized; Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome deletion; epilepsy, generalized; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes, type 2; atherosclerosis, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, generalized; epilepsy, reflex Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, generalized; epilepsy, reflex in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, generalized; seizures, febrile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, generalized; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
generalized epilepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease generalized epilepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, generalized; epilepsy, tonic-clonic Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, generalized; epilepsy, tonic-clonic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
generalized epimerase-deficiency galactosemia Gene Set From GAD Gene-Disease Associations genes associated with the disease generalized epimerase-deficiency galactosemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsy, idiopathic generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsy, idiopathic generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
epilepsies, partial; epilepsy, generalized; seizures, febrile Gene Set From GAD Gene-Disease Associations genes associated with the disease epilepsies, partial; epilepsy, generalized; seizures, febrile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lipids; atherosclerosis, generalized Gene Set From GAD Gene-Disease Associations genes associated with the disease lipids; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
generalized Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term generalized in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Generalized seizures_Brain_GSE6614 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Generalized seizures_Brain_GSE6614 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Epilepsy (generalized) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Epilepsy (generalized) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
generalized hypotonia Gene Set From GWASdb SNP-Phenotype Associations genes associated with the generalized hypotonia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
generalized amyloid deposition Gene Set From GWASdb SNP-Phenotype Associations genes associated with the generalized amyloid deposition phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
moderate generalized osteoporosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the moderate generalized osteoporosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
generalized abnormality of skin Gene Set From GWASdb SNP-Phenotype Associations genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
generalized osteosclerosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the generalized osteosclerosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
eeg with generalized epileptiform discharges Gene Set From HPO Gene-Disease Associations genes associated with the eeg with generalized epileptiform discharges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized osteosclerosis Gene Set From HPO Gene-Disease Associations genes associated with the generalized osteosclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized limb muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the generalized limb muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hyperreflexia Gene Set From HPO Gene-Disease Associations genes associated with the generalized hyperreflexia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized tonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized tonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized abnormality of skin Gene Set From HPO Gene-Disease Associations genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized bone demineralization Gene Set From HPO Gene-Disease Associations genes associated with the generalized bone demineralization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized morning stiffness Gene Set From HPO Gene-Disease Associations genes associated with the generalized morning stiffness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized muscle hypertrophy Gene Set From HPO Gene-Disease Associations genes associated with the generalized muscle hypertrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized amyotrophy Gene Set From HPO Gene-Disease Associations genes associated with the generalized amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized arterial tortuosity Gene Set From HPO Gene-Disease Associations genes associated with the generalized arterial tortuosity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized opacification of the cornea Gene Set From HPO Gene-Disease Associations genes associated with the generalized opacification of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the generalized hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hyperpigmentation Gene Set From HPO Gene-Disease Associations genes associated with the generalized hyperpigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hirsutism Gene Set From HPO Gene-Disease Associations genes associated with the generalized hirsutism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hypopigmentation of hair Gene Set From HPO Gene-Disease Associations genes associated with the generalized hypopigmentation of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized aminoaciduria Gene Set From HPO Gene-Disease Associations genes associated with the generalized aminoaciduria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized seborrheic dermatitis Gene Set From HPO Gene-Disease Associations genes associated with the generalized seborrheic dermatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized myoclonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized myoclonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized arterial calcification Gene Set From HPO Gene-Disease Associations genes associated with the generalized arterial calcification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized edema Gene Set From HPO Gene-Disease Associations genes associated with the generalized edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
eeg with generalized slow activity Gene Set From HPO Gene-Disease Associations genes associated with the eeg with generalized slow activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intermittent generalized erythematous papular rash Gene Set From HPO Gene-Disease Associations genes associated with the intermittent generalized erythematous papular rash phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized tonic-clonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized tonic-clonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized neonatal hypotonia Gene Set From HPO Gene-Disease Associations genes associated with the generalized neonatal hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hyperkeratosis Gene Set From HPO Gene-Disease Associations genes associated with the generalized hyperkeratosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized osteoporosis with pathologic fractures Gene Set From HPO Gene-Disease Associations genes associated with the generalized osteoporosis with pathologic fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the generalized muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hypopigmentation Gene Set From HPO Gene-Disease Associations genes associated with the generalized hypopigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized papillary lesions Gene Set From HPO Gene-Disease Associations genes associated with the generalized papillary lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized hypotonia due to defect at the neuromuscular junction Gene Set From HPO Gene-Disease Associations genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized distal tubular acidosis Gene Set From HPO Gene-Disease Associations genes associated with the generalized distal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized cerebral atrophy/hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized clonic seizures Gene Set From HPO Gene-Disease Associations genes associated with the generalized clonic seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized muscular appearance from birth Gene Set From HPO Gene-Disease Associations genes associated with the generalized muscular appearance from birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized joint laxity Gene Set From HPO Gene-Disease Associations genes associated with the generalized joint laxity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
congenital, generalized hypertrichosis Gene Set From HPO Gene-Disease Associations genes associated with the congenital, generalized hypertrichosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized lipodystrophy Gene Set From HPO Gene-Disease Associations genes associated with the generalized lipodystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized amyloid deposition Gene Set From HPO Gene-Disease Associations genes associated with the generalized amyloid deposition phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Epilepsy, Generalized Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Epilepsy, Generalized phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
epilepsy, idiopathic generalized, susceptibility to, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, idiopathic generalized, susceptibility to, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, 10} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, 10} phenotype from the curated OMIM Gene-Disease Associations dataset.
generalized epilepsy and paroxysmal dyskinesia Gene Set From OMIM Gene-Disease Associations genes associated with the generalized epilepsy and paroxysmal dyskinesia phenotype from the curated OMIM Gene-Disease Associations dataset.
epilespy, generalized, with febrile seizures plus, type 8 Gene Set From OMIM Gene-Disease Associations genes associated with the epilespy, generalized, with febrile seizures plus, type 8 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 9} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, suscpetibility to, 12} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, suscpetibility to, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.
generalized epilepsy with febrile seizures plus, type 9 Gene Set From OMIM Gene-Disease Associations genes associated with the generalized epilepsy with febrile seizures plus, type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, generalized, with febrile seizures plus, type 5, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 3} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.
thyrotropin-releasing hormone resistance, generalized Gene Set From OMIM Gene-Disease Associations genes associated with the thyrotropin-releasing hormone resistance, generalized phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, idiopathic generalized, susceptibility to 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, idiopathic generalized, susceptibility to 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 7 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 6 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 4 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, generalized, with febrile seizures plus, type 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, generalized, with febrile seizures plus, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
?lipodystrophy, congenital generalized, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the ?lipodystrophy, congenital generalized, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
epidermolysis bullosa, generalized atrophic benign Gene Set From OMIM Gene-Disease Associations genes associated with the epidermolysis bullosa, generalized atrophic benign phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, congenital generalized, type 1 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, congenital generalized, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
hypertrichosis, congenital generalized Gene Set From OMIM Gene-Disease Associations genes associated with the hypertrichosis, congenital generalized phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy idiopathic generalized, susceptibility to, 8} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy idiopathic generalized, susceptibility to, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.
hypertrichosis terminalis, generalized, with or without gingival hyperplasia Gene Set From OMIM Gene-Disease Associations genes associated with the hypertrichosis terminalis, generalized, with or without gingival hyperplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, congenital generalized, type 2 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, congenital generalized, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
lipodystrophy, congenital generalized, type 4 Gene Set From OMIM Gene-Disease Associations genes associated with the lipodystrophy, congenital generalized, type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, idiopathic generalized, susceptibility to, 11} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, idiopathic generalized, susceptibility to, 11} phenotype from the curated OMIM Gene-Disease Associations dataset.
arterial calcification, generalized, of infancy, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the arterial calcification, generalized, of infancy, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
arterial calcification, generalized, of infancy, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the arterial calcification, generalized, of infancy, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
Generalized Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Myoclonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Myoclonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Enlarged Lymph Nodes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Enlarged Lymph Nodes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Anxiety Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Anxiety Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Amyotrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Generalized Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Hypopigmentation Of Hair Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Hypopigmentation Of Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aggressive Periodontitis, Generalized Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Aggressive Periodontitis, Generalized in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Glycogen Storage Disease Of Infants Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Glycogen Storage Disease Of Infants in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Vitiligo Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Vitiligo in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Clonic Seizures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Clonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Limb Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Limb Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Cerebral Atrophy/Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Cerebral Atrophy/Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Epilepsy With Febrile Seizures Plus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Generalized Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Chronic Periodontitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Chronic Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Osteoarthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Osteoarthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Thyroid Hormone Resistance Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Thyroid Hormone Resistance in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anhidrosis, Familial Generalized, With Abnormal Or Absent Sweat Glands Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anhidrosis, Familial Generalized, With Abnormal Or Absent Sweat Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Pustular Psoriasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Pustular Psoriasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anxiety Generalized Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anxiety Generalized in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Episodic Generalized Hypotonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Episodic Generalized Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Tetanus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Tetanus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Morphea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Morphea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Seborrheic Dermatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Seborrheic Dermatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Convulsive Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Convulsive Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Nonconvulsive Seizure Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Nonconvulsive Seizure Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symptomatic Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symptomatic Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Periodontitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Generalized Exanthematous Pustulosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Generalized Exanthematous Pustulosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Osteoporosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Osteoporosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Obesity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Obesity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Osteopenia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Osteopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myasthenia Gravis, Generalized Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myasthenia Gravis, Generalized in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Myotonia Of Thomsen Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Myotonia Of Thomsen in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Becker Generalized Myotonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Becker Generalized Myotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Abnormality Of Skin Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Abnormality Of Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Dystrophic Epidermolysis Bullosa Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Dystrophic Epidermolysis Bullosa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Generalized Recessive Dystrophic Epidermolysis Bullosa Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Generalized Recessive Dystrophic Epidermolysis Bullosa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Tonic-Clonic Seizures With Focal Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Tonic-Clonic Seizures With Focal Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyroid Hormone Resistance, Generalized, Autosomal Recessive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Hormone Resistance, Generalized, Autosomal Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Histiocytosis, Generalized Eruptive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Histiocytosis, Generalized Eruptive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Distal Tubular Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Distal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Generalized Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Generalized Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Epilepsy And Paroxysmal Dyskinesia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Epilepsy And Paroxysmal Dyskinesia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Generalized Lipodystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Generalized Lipodystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Epilepsy With Febrile Seizures Plus, 7 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Epilepsy With Febrile Seizures Plus, 7 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Social Phobia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Social Phobia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Hypotrichosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Hypotrichosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thyrotropin-Releasing Hormone Resistance, Generalized Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thyrotropin-Releasing Hormone Resistance, Generalized in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Hyperpigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hyperpigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Muscle Weakness, Ctcae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscle Weakness, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Absence Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Absence Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hirsutism Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hirsutism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Generalized Epileptiform Discharges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Generalized Epileptiform Discharges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Weakness Of Limb Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Weakness Of Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Tonic Seizures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Tonic Seizures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Neonatal Hypotonia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Neonatal Hypotonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Irregular Generalized Spike And Wave Complexes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Irregular Generalized Spike And Wave Complexes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Muscular Appearance From Birth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscular Appearance From Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hyperkeratosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hyperkeratosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Joint Laxity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Joint Laxity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Bone Demineralization Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Bone Demineralization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Amyloid Deposition Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Amyloid Deposition in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hypertrichosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypertrichosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Pruritus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Pruritus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Morning Stiffness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Morning Stiffness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Tonic-Clonic Seizures On Awakening Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Tonic-Clonic Seizures On Awakening in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Edema, Ctcae Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Edema, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Generalized Slow Activity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Generalized Slow Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hypotonia Due To Defect At The Neuromuscular Junction Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypotonia Due To Defect At The Neuromuscular Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Osteosclerosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Osteosclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Generalized Osteoporosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Generalized Osteoporosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Headache Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Headache in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Aminoaciduria Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Aminoaciduria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Bronze Hyperpigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Bronze Hyperpigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Muscle Wasting Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscle Wasting in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hyperreflexia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hyperreflexia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Arterial Tortuosity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Arterial Tortuosity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Eeg With Generalized Polyspikes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Eeg With Generalized Polyspikes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Arterial Calcification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Arterial Calcification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Spasms Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Spasms in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Hypopigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Hypopigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Papillary Lesions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Papillary Lesions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Anhidrosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Anhidrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Microdontia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Microdontia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intermittent Generalized Erythematous Papular Rash Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intermittent Generalized Erythematous Papular Rash in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Ichthyosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Ichthyosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Reticulate Brown Pigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Reticulate Brown Pigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Muscle Hypertrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscle Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
generalized edema Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the generalized edema phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Congenital generalized lipodystrophy Gene Set From WikiPathways Pathways 2024 proteins participating in the Congenital generalized lipodystrophy pathway from the WikiPathways Pathways 2024 dataset.
Complete generalized lipodystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Complete generalized lipodystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Congenital generalized lipodystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Idiopathic generalized epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Generalized epilepsy with febrile seizures plus from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Idiopathic generalized epilepsy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized anxiety disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized anxiety disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epilepsy with generalized tonic-clonic seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epilepsy with generalized tonic-clonic seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized atherosclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized atherosclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Persistent generalized lymphadenopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Persistent generalized lymphadenopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Acquired generalized lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Acquired generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complete generalized lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complete generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized lymphatic anomaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized lymphatic anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epidermolysis bullosa simplex generalized type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epidermolysis bullosa simplex generalized type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bilateral generalized polymicrogyria Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bilateral generalized polymicrogyria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital generalized lipodystrophy type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital generalized lipodystrophy type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Generalized epilepsy with febrile seizures plus 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Generalized epilepsy with febrile seizures plus 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic generalized epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic generalized epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Idiopathic generalized epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital generalized lipodystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital generalized lipodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized juvenile polyposis/juvenile polyposis coli Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized juvenile polyposis/juvenile polyposis coli phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized dominant dystrophic epidermolysis bullosa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized dominant dystrophic epidermolysis bullosa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized pustular psoriasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized pustular psoriasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized hypotonia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized hypotonia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized epilepsy-paroxysmal dyskinesia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized epilepsy-paroxysmal dyskinesia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized-onset seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized-onset seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized hypopigmentation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized hypopigmentation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized myoclonic seizure Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized myoclonic seizure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SCN2A-related generalized epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SCN2A-related generalized epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized hyperreflexia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized hyperreflexia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset generalized dyskinesia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset generalized dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized hypertrichosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized hypertrichosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized choriocapillaris dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized choriocapillaris dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Response to antiepileptic drugs in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to antiepileptic drugs in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to valproic acid in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to valproic acid in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to lamotrigine in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to lamotrigine in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to levetiracetam in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to levetiracetam in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to lamotrigine and valproic acid in genetic generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to lamotrigine and valproic acid in genetic generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Generalized epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Generalized epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

generalized dystonia Gene Set

generalized dystonia Gene Set

generalized dystonia Gene Set

Generalized Dystonia Gene Set

Generalized dystonia Gene Set

Generalized dystonia Gene Set

Generalized dystonia Gene Set

Early-onset generalized limb-onset dystonia Gene Set

Hypermanganesemia with dystonia, polycythemia and cirrhosis Gene Set

Dystonia 24 Gene Set

Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive Gene Set

Autosomal dominant torsion dystonia 4 Gene Set

Dystonia 12 Gene Set

Dystonia 10 Gene Set

Dystonia 16 Gene Set

Dystonia 18 Gene Set

Myoclonic dystonia Gene Set

Juvenile-onset dystonia Gene Set

Dystonia 25 Gene Set

Dystonia 6, torsion Gene Set

Dystonia 5, Dopa-responsive type Gene Set

Dystonia 3, torsion, X-linked Gene Set

Dystonia 1 Gene Set

Infantile Parkinsonism-dystonia Gene Set

Parkinsonism-Dystonia, Infantile Gene Set

Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set

Dystonia musculorum deformans type 2 Gene Set

Dystonia 13, Torsion Gene Set

Dystonia musculorum deformans type 1 Gene Set

Torsion dystonia 7 Gene Set

Dystonia 17, Torsion, Autosomal Recessive Gene Set

Dystonia 15, myoclonic Gene Set

LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene Set

Dystonia 12 Gene Set

Myoclonic dystonia Gene Set

Familial paroxysmal dystonia Gene Set

Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene Set

Hypermanganesemia with Dystonia Polycythemia and Cirrhosis Gene Set

Juvenile-onset dystonia Gene Set

Dystonia 3, Torsion, X-Linked Gene Set

Dystonia 6, torsion Gene Set

Dystonia, Dopa-responsive Gene Set

Cervical Dystonia, Primary Gene Set

Dystonia Gene Set

dystonia Gene Set

deafness dystonia syndrome Gene Set

dystonia Gene Set

dystonia Gene Set

cranio-facial dystonia Gene Set

focal dystonia Gene Set

deafness dystonia syndrome Gene Set

dystonia, primary torsion Gene Set

complex regional pain syndromes; dystonia; Gene Set

myoclonus dystonia Gene Set

dystonia; Gene Set

idiopathic torsion dystonia Gene Set

dystonia, primary Gene Set

chromosome aberrations; chromosome deletion; dystonia; myoclonus Gene Set

cervical dystonia Gene Set

dystonia, cervical Gene Set

dystonia, focal Gene Set

blepharospasm; dystonia; dystonic disorders; torticollis Gene Set

dystonia Gene Set

dystonia, early onset primary Gene Set

akathisia, drug-induced; dystonia Gene Set

dystonia; psychomotor disorders; syndrome Gene Set

focal dystonia Gene Set

dystonia Gene Set

Musician's dystonia Gene Set

craniofacial dystonia Gene Set

limb dystonia Gene Set

axial dystonia Gene Set

oromandibular dystonia Gene Set

dystonia Gene Set

paroxysmal dystonia Gene Set

laryngeal dystonia Gene Set

torsion dystonia Gene Set

focal dystonia Gene Set

Dystonia Musculorum Deformans Gene Set